Total knee arthroplasty
Conditions
Interventions
Control group:The cocktail without Diprospan solution was injected around the joint
Experimental group 1:A cocktail containing 1ml of Diprospan solution was injected around the joint
Experimental group 2:A cocktail containing 2ml of Diprospan solution was injected around the joint
Experimental group 3:A cocktail containing 3ml of Diprospan solution was injected around the joint
Sponsors
The First Affiliated Hospital of Xinjiang Medical University
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1. Patients with TKA operation indications who underwent primary total knee arthroplasty; 2. Aged 18 to 80 years; 3. The patient volunteered and signed the informed consent.
Exclusion criteria
Exclusion criteria: 1. Past or recent history of taking opioids; 2. Patients who are unwilling or unable to sign the informed consent, have mental illness, and are unable to complete the postoperative pain score; 3. There was a history of opioid, glucocorticoid or sulfonamide allergy before operation; 4. Patients who cannot tolerate anesthesia and surgery; 5. Patients who are participating in other clinical trials; 6. Researchers think that other reasons are not suitable for clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| visual analogue scale;American knee society score;range of motion;forget joint score; | — |
Countries
China
Contacts
Public ContactWang Yang
The First Affiliated Hospital of Xinjiang Medical University
Outcome results
None listed